Canonical Allele Identifier: PA2829375018
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 3118176
ClinVar RCV Id: RCV004412557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Ala1617Val
CA348592352
NM_002299.3:c.4850C>T